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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425625생성일: 2026년 10월 26일

2-Hydroxyethyl Methacrylate → 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate

https://huagongshe.com/reaction/1425625

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydroxyethyl MethacrylateHCID 13360—
반응물(7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoateHCID 14645478—
반응물2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
반응물1-Cyclohexyloxyethyl methacrylateHCID 22995281—
용매Methyl Isobutyl KetoneHCID 7909—
용매HeptaneHCID 8900—
생성물1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylateHCID 86643210—

반응 단계

Into a 500 ml-volume three-neck flask, 76.4 g (0.36 mol) of 1-cyclohexyloxyethyl methacrylate, 35.3 g (0.18 mol) of 3,4-epoxycyclohexylmethyl methacrylate (Cyclomer M100, produced by Daicel Chemical Industries, Ltd.), 7.8 g (0.06 mol) of 2-hydroxyethyl methacrylate and 300 ml of methyl isobutyl ketone were charged. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) was added thereto as a radical polymerization initiator, and polymerization was allowed to proceed at 80° C. for 6 hours in a nitrogen stream. The reaction solution was cooled and then poured in a large amount of heptane to precipitate a polymer. The crystal was collected by filtration and dissolved in diethylene glycol dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-5 (1-cyclohexyloxyethyl methacrylate/3,4-epoxycyclohexylmethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08932800B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-4698e2394c2b4f6990241ab9f73e7f12
출처 메모uspto-grants-2015_01